Structure of PDB 4njk Chain A Binding Site BS02
Receptor Information
>4njk Chain A (length=209) Species:
395019
(Burkholderia multivorans ATCC 17616) [
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TYAVKEIFYTLQGEGANAGRPAVFCRFAGCNLWSGREEDRAQAVCRFCDT
DFVGTDGENGGKFKDADALVATIAGLWPAGEAHRFVVCTGGEPMLQLDQP
LVDALHAAGFGIAIETNGSLPVLESIDWICVSPKADAPLVVTKGNELKVV
IPQDNQRLADYAKLDFEYFLVQPMDGPSRDLNTKLAIDWCKRHPQWRLSM
QTHKYLNIP
Ligand information
Ligand ID
SAM
InChI
InChI=1S/C15H22N6O5S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/t7-,8+,10+,11+,14+,27-/m0/s1
InChIKey
MEFKEPWMEQBLKI-FCKMPRQPSA-N
SMILES
Software
SMILES
CACTVS 3.341
C[S@@+](CC[C@H](N)C([O-])=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
C[S+](CCC(C(=O)[O-])N)CC1C(C(C(O1)n2cnc3c2ncnc3N)O)O
CACTVS 3.341
C[S+](CC[CH](N)C([O-])=O)C[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
C[S@@+](CC[C@@H](C(=O)[O-])N)C[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)O
ACDLabs 10.04
[O-]C(=O)C(N)CC[S+](C)CC3OC(n2cnc1c(ncnc12)N)C(O)C3O
Formula
C15 H22 N6 O5 S
Name
S-ADENOSYLMETHIONINE
ChEMBL
CHEMBL1235831
DrugBank
ZINC
PDB chain
4njk Chain A Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
4njk
Radical SAM enzyme QueE defines a new minimal core fold and metal-dependent mechanism.
Resolution
1.911 Å
Binding residue
(original residue number in PDB)
F48 C49 D50 T51 T90 G91 G92 E93 E116 T117 N118 S133 K135 V151 M175 D176 Q202
Binding residue
(residue number reindexed from 1)
F47 C48 D49 T50 T89 G90 G91 E92 E115 T116 N117 S132 K134 V150 M174 D175 Q201
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F25 C31 C46 C49 D50 T51 E116 H204
Catalytic site (residue number reindexed from 1)
F24 C30 C45 C48 D49 T50 E115 H203
Enzyme Commision number
4.3.99.3
: 7-carboxy-7-deazaguanine synthase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0016829
lyase activity
GO:0016840
carbon-nitrogen lyase activity
GO:0042802
identical protein binding
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
GO:0051536
iron-sulfur cluster binding
GO:0051539
4 iron, 4 sulfur cluster binding
GO:1904047
S-adenosyl-L-methionine binding
Biological Process
GO:0008616
queuosine biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4njk
,
PDBe:4njk
,
PDBj:4njk
PDBsum
4njk
PubMed
24362703
UniProt
A0A0H3KB22
|QUEE_BURM1 7-carboxy-7-deazaguanine synthase (Gene Name=queE)
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